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氟掺杂氧化锡电极上原子层沉积的AlO薄膜:稳定性和阻隔性能。

Atomic layer deposited films of AlO on fluorine-doped tin oxide electrodes: stability and barrier properties.

作者信息

Krýsová Hana, Neumann-Spallart Michael, Tarábková Hana, Janda Pavel, Kavan Ladislav, Krýsa Josef

机构信息

J. Heyrovsky Institute of Physical Chemistry, Czech Academy of Sciences, Dolejškova 2155/3, 182 23 Prague 8, Czech Republic.

Department of Inorganic Technology, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech Republic.

出版信息

Beilstein J Nanotechnol. 2021 Jan 5;12:24-34. doi: 10.3762/bjnano.12.2. eCollection 2021.

DOI:10.3762/bjnano.12.2
PMID:33489664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7801786/
Abstract

AlO layers were deposited onto electrodes by atomic layer deposition. Solubility and electron-transport blocking were tested. Films deposited onto fluorine-doped tin oxide (FTO, F:SnO/glass) substrates blocked electron transfer to redox couples (ferricyanide/ferrocyanide) in aqueous media. However, these films were rapidly dissolved in 1 M NaOH (≈100 nm/h). The dissolution was slower in 1 M HSO (1 nm/h) but after 24 h the blocking behaviour was entirely lost. The optimal stability was reached at pH 7.2 where no changes were found up to 24 h and even after 168 h of exposure the changes in the blocking behaviour were still minimal. This behaviour was also observed for protection against direct reduction of FTO.

摘要

通过原子层沉积将AlO层沉积在电极上。测试了溶解度和电子传输阻断性能。沉积在氟掺杂氧化锡(FTO,F:SnO/玻璃)衬底上的薄膜在水性介质中阻断了电子向氧化还原对(铁氰化物/亚铁氰化物)的转移。然而,这些薄膜在1 M NaOH中迅速溶解(约100 nm/h)。在1 M HSO中溶解较慢(1 nm/h),但24小时后阻断行为完全丧失。在pH 7.2时达到最佳稳定性,在24小时内未发现变化,甚至在暴露168小时后,阻断行为的变化仍然很小。对于防止FTO直接还原也观察到了这种行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/6adc62546f56/Beilstein_J_Nanotechnol-12-24-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/9988f2646bc6/Beilstein_J_Nanotechnol-12-24-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/40549230d05b/Beilstein_J_Nanotechnol-12-24-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/94b789dfad01/Beilstein_J_Nanotechnol-12-24-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/01cf031a2a78/Beilstein_J_Nanotechnol-12-24-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/ddef04ba8ff9/Beilstein_J_Nanotechnol-12-24-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/c7315611e2c4/Beilstein_J_Nanotechnol-12-24-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/ca574f6f827e/Beilstein_J_Nanotechnol-12-24-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/6adc62546f56/Beilstein_J_Nanotechnol-12-24-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/9988f2646bc6/Beilstein_J_Nanotechnol-12-24-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/1e675d28f32d/Beilstein_J_Nanotechnol-12-24-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/40549230d05b/Beilstein_J_Nanotechnol-12-24-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/94b789dfad01/Beilstein_J_Nanotechnol-12-24-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/01cf031a2a78/Beilstein_J_Nanotechnol-12-24-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/ddef04ba8ff9/Beilstein_J_Nanotechnol-12-24-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/c7315611e2c4/Beilstein_J_Nanotechnol-12-24-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/ca574f6f827e/Beilstein_J_Nanotechnol-12-24-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b611/7801786/6adc62546f56/Beilstein_J_Nanotechnol-12-24-g010.jpg

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